Evidence map›Paper›PMID 32812754›Full record

ReviewChemical reviews2020

Enzymatic Noncovalent Synthesis.

Hongjian He, Weiyi Tan, Jiaqi Guo, Meihui Yi, Adrianna N Shy, Bing Xu

Abstract readReview
In one paragraph

Review in Chemical reviews, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

54 citing papers in PubMed.

  1. Article
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  4. Materials today. Bio · 2026
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  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
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  12. Synzymes: The Future of Modern Enzyme Engineering.Applied biochemistry and biotechnology · 2025
    Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Hongjian HeDepartment of Chemistry, Brandeis University, 415 South Street, Waltham, Massachusetts 02454, United States.
Weiyi TanDepartment of Chemistry, Brandeis University, 415 South Street, Waltham, Massachusetts 02454, United States.
Jiaqi GuoDepartment of Chemistry, Brandeis University, 415 South Street, Waltham, Massachusetts 02454, United States.
Meihui YiDepartment of Chemistry, Brandeis University, 415 South Street, Waltham, Massachusetts 02454, United States.
Adrianna N ShyDepartment of Chemistry, Brandeis University, 415 South Street, Waltham, Massachusetts 02454, United States.
Bing XuDepartment of Chemistry, Brandeis University, 415 South Street, Waltham, Massachusetts 02454, United States.ORCID 0000-0002-4639-387X

Funding

Subcellular Enzyme-instructed self-assembly for molecular anticancer nanomedicinesR01CA142746 · NCI · BRANDEIS UNIVERSITY · PI Bing Xu · 2010 to 2026
$6.4M
Exploring enzyme-instructed self-assembly (EISA) for targeting osteoblastic metastasis of prostate cancerR21CA252364 · NCI · BRANDEIS UNIVERSITY · PI HSIEH, JER-TSONG, XU, BING · 2020 to 2020
$430k
NCI NIH HHS R01 CA142746NCI NIH HHS R21 CA252364
6 · The paper itself

Abstract

Enzymatic reactions and noncovalent (i.e., supramolecular) interactions are two fundamental nongenetic attributes of life. Enzymatic noncovalent synthesis (ENS) refers to a process where enzymatic reactions control intermolecular noncovalent interactions for spatial organization of higher-order molecular assemblies that exhibit emergent properties and functions. Like enzymatic covalent synthesis (ECS), in which an enzyme catalyzes the formation of covalent bonds to generate individual molecules, ENS is a unifying theme for understanding the functions, morphologies, and locations of molecular ensembles in cellular environments. This review intends to provide a summary of the works of ENS within the past decade and emphasize ENS for functions. After comparing ECS and ENS, we describe a few representative examples where nature uses ENS, as a rule of life, to create the ensembles of biomacromolecules for emergent properties/functions in a myriad of cellular processes. Then, we focus on ENS of man-made (synthetic) molecules in cell-free conditions, classified by the types of enzymes. After that, we introduce the exploration of ENS of man-made molecules in the context of cells by discussing intercellular, peri/intracellular, and subcellular ENS for cell morphogenesis, molecular imaging, cancer therapy, and other applications. Finally, we provide a perspective on the promises of ENS for developing molecular assemblies/processes for functions. This review aims to be an updated introduction for researchers who are interested in exploring noncovalent synthesis for developing molecular science and technologies to address societal needs.

Indexed as

AnimalsEnzymesHumansEnzymes

Identifiers

PMID32812754
PMCPMC7530130

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.